Welcome to chemicalbook!
+1 (818) 612-2111
RFQ
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

RFQ
skype
MY Account
Top
Postion:Product Catalog >Tryptophan EP Impurity K
Tryptophan EP Impurity K
  • Tryptophan EP Impurity K
  • Tryptophan EP Impurity K
  • Tryptophan EP Impurity K
  • Tryptophan EP Impurity K
  • Tryptophan EP Impurity K

Tryptophan EP Impurity K NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Tryptophan EP Impurity K CAS No.: 149724-31-2
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

Tryptophan EP Impurity K


Article illustration

Product Information

  • Product Code:T057011

  • English Name:Tryptophan EP Impurity K

  • English Alias:(S)-3-(2-((1H-indol-3-yl)methyl)-1H-indol-3-yl)-2-aminopropanoic acid

  • CAS No.:149724-31-2

  • Molecular Formula:C₂₀H₁₉N₃O₂

  • Molecular Weight:333.38

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), HRMS, and elemental analysis, compliant with EP (European Pharmacopoeia) impurity standards for Tryptophan quality control.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.3% in aqueous solution (pH 5-7) within 6 months.

Applications

  • Quality Control Testing:Used for HPLC and LC-MS detection of EP Impurity K in Tryptophan API and formulations, controlling content to meet EP standards (≤0.1%).

  • Process Optimization Research:Monitors impurity formation during Tryptophan synthesis, reducing generation by >50% by adjusting condensation temperature (e.g., 70-80℃) and reaction time.

  • Method Validation:Serves as an EP standard for developing impurity detection methods, verifying HPLC resolution (≥2.5) and LOD (0.01 ng/mL).

Background Description

Tryptophan, an essential amino acid, is used in nutritional supplements and pharmaceutical intermediates. Impurity K, specified by EP, may originate from alkylation side reactions of the indole ring or raw material residues during synthesis. Its bis-indole system may affect Tryptophan's stability and biological activity. With stricter EMA enforcement of EP standards, studying such officially designated impurities is crucial for drug registration and manufacturing.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 3.5 minutes, with LOD of 0.003 ng/mL for EP-compliant trace analysis.

  • Formation Mechanism:Formed by reaction of 3-indolecarboxaldehyde with Tryptophan under acidic conditions (e.g., acetic acid catalysis); optimizing catalyst dosage and solvent polarity (e.g., ethanol-water system) inhibits side reactions.

  • Safety Evaluation:In vitro cytotoxicity shows IC₅₀ of 178.6 μM against C2C12 myoblasts (Tryptophan IC₅₀=21.3 μM), with low toxicity but requiring ≤0.1% limit. Long-term stability testing is ongoing to monitor degradation under different pH conditions.

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.

This product is intended for laboratory use only!

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 







Company Profile Introduction

-

You may like

Recommended supplier

Product name Price   Suppliers Update time
$0.00/5mg
VIP1Y
Guangzhou Tosun Pharmaceutical Ltd
2024-12-20
$2500.00/25mg
VIP2Y
R&D Scientific Inc.
2025-09-16
$0.00/10mg
VIP2Y
ShenZhen H&D Pharmaceutical Technology Co., LTD
2024-06-28
INQUIRY